TY - JOUR
T1 - How Ag Nanospheres Are Transformed into AgAu Nanocages
AU - Moreau, Liane M.
AU - Schurman, Charles A.
AU - Kewalramani, Sumit
AU - Shahjamali, Mohammad M.
AU - Mirkin, Chad A.
AU - Bedzyk, Michael J.
N1 - Funding Information:
C.A.S., S.K., C.A.M., and M.J.B. acknowledge support by the AFOSR under Award FA9550-11-1-0275. C.A.M. and L.M.M. acknowledge support from the Vannevar Bush Faculty Fellowship program sponsored by the Basic Research Office of the Assistant Secretary of Defense for Research and Engineering, and funded by the Office of Naval Research through grant N00014-15-1-0043. L.M.M. was also funded by a National Defense Science and Engineering Graduate (NDSEG) fellowship. S.K. was partially funded by DOE-BES (DE-FG02-08ER46539). M.M.S. acknowledges the SINGA fellowship by Singapore Agency for Science, Technology and Research (A*STAR) and a Postdoctoral Fellowship supported by the School of Materials Science and Engineering, Nanyang Technological University. This work made use of the EPIC facility of Northwestern University’s NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the MRSEC program (NSF DMR-1121262) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN. Metal analysis was performed at the Northwestern University Quantitative Bioelement Imaging Center (QBIC) supported by NASA Ames Research Center NNA06CB93G. SAXS experiments were performed at the APS DND-CAT 5ID-D beamline, which is supported through E. I. duPont de Nemours & Co., Northwestern University (NU), The Dow Chemical Co., and the NSF funded MRSEC at NU. EXAFS and XRF experiments were performed at the APS 10BM-B beamline (MR-CAT), which is supported by the Department of Energy and the MRCAT member institutions. Use of the APS was supported by DOE-BES (DE-AC02-06CH11357). We thank Steven Weigand of DND-CAT for assistance with the SAXS setup and data reduction, Joshua Wright of MR-CAT for assistance with the EXAFS setup and Keith MacRenaris of QBIC for assistance with ICP-MS.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/9/6
Y1 - 2017/9/6
N2 - Bimetallic hollow, porous noble metal nanoparticles are of broad interest for biomedical, optical and catalytic applications. The most straightforward method for preparing such structures involves the reaction between HAuCl4 and well-formed Ag particles, typically spheres, cubes, or triangular prisms, yet the mechanism underlying their formation is poorly understood at the atomic scale. By combining in situ nanoscopic and atomic-scale characterization techniques (XAFS, SAXS, XRF, and electron microscopy) to follow the process, we elucidate a plausible reaction pathway for the conversion of citrate-capped Ag nanospheres to AgAu nanocages; importantly, the hollowing event cannot be explained by the nanoscale Kirkendall effect, nor by Galvanic exchange alone, two processes that have been previously proposed. We propose a modification of the bulk Galvanic exchange process that takes into account considerations that can only occur with nanoscale particles. This nanoscale Galvanic exchange process explains the novel morphological and chemical changes associated with the typically observed hollowing process.
AB - Bimetallic hollow, porous noble metal nanoparticles are of broad interest for biomedical, optical and catalytic applications. The most straightforward method for preparing such structures involves the reaction between HAuCl4 and well-formed Ag particles, typically spheres, cubes, or triangular prisms, yet the mechanism underlying their formation is poorly understood at the atomic scale. By combining in situ nanoscopic and atomic-scale characterization techniques (XAFS, SAXS, XRF, and electron microscopy) to follow the process, we elucidate a plausible reaction pathway for the conversion of citrate-capped Ag nanospheres to AgAu nanocages; importantly, the hollowing event cannot be explained by the nanoscale Kirkendall effect, nor by Galvanic exchange alone, two processes that have been previously proposed. We propose a modification of the bulk Galvanic exchange process that takes into account considerations that can only occur with nanoscale particles. This nanoscale Galvanic exchange process explains the novel morphological and chemical changes associated with the typically observed hollowing process.
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U2 - 10.1021/jacs.7b06724
DO - 10.1021/jacs.7b06724
M3 - Article
C2 - 28800390
AN - SCOPUS:85028929568
SN - 0002-7863
VL - 139
SP - 12291
EP - 12298
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 35
ER -